Cargando…
Detection of melanocyte lineage-specific genes in vitiligo lesions
Vitiligo is an acquired pigmentary disorder characterized by the loss of skin color and functional melanocytes. The pathogenesis of vitiligo remains unclear, which means that effective clinical treatment is difficult. However, if melanocyte linkage-specific genes are identified in vitiligo lesions,...
Autores principales: | Xu, Wanwen, Wang, Xiong |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6489045/ https://www.ncbi.nlm.nih.gov/pubmed/31086580 http://dx.doi.org/10.3892/etm.2019.7496 |
Ejemplares similares
-
VITILIGO AND THE MELANOCYTE RESERVOIR
por: Falabella, Rafael
Publicado: (2009) -
Mechanisms of melanocyte death in vitiligo
por: Chen, Jianru, et al.
Publicado: (2020) -
Antibodies to normal human melanocytes in vitiligo
Publicado: (1983) -
Imiquimod induced vitiligo‐like lesions—A consequence of modified melanocyte function
por: Yu, Haiyan, et al.
Publicado: (2021) -
ZMIZ1 promotes the proliferation and migration of melanocytes in vitiligo
por: Li, Meng, et al.
Publicado: (2020)